Canonical Allele Identifier: CA2505161591
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782214A>C , CM000672.2:g.94782214A>C GRCh38
NC_000010.10:g.96541971A>C , CM000672.1:g.96541971A>C GRCh37
NC_000010.9:g.96531961A>C NCBI36
NG_008384.2:g.24509A>C
NG_008384.3:g.24534A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+217A>C MANE Select ENSP00000360372.3:n.819+217A>C
ENST00000645461.1:n.1872+217A>C
ENST00000371321.7:c.819+217A>C ENSP00000360372.3:n.819+217A>C
ENST00000464755.1:c.1582+217A>C ENSP00000483243.1:n.1582+217A>C
NM_000769.2:c.819+217A>C NP_000760.1:n.819+217A>C
NM_000769.4:c.819+217A>C MANE Select NP_000760.1:n.819+217A>C
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